摘要
以γ-聚谷氨酸(PGA)和壳聚糖(CS)作为基材,聚乙烯吡咯烷酮(PVP)、三聚磷酸钠(STPP)作为稳定剂和交联剂制备缓释姜黄素的纳米颗粒。通过比较不同浓度比配方下的姜黄素在纳米颗粒中的包埋率、结构表征及红外光谱分析确定最优配方;采用动态透析法考察包埋姜黄素的纳米颗粒在2种pH值中的体外释放特性。结果表明得到姜黄素纳米颗粒最优配方:姜黄素浓度0.26mg/mL、PGA浓度0.2%、STPP浓度0.2%、PVP浓度0.1%、CS浓度0.02%(以100mL水溶液计);纳米颗粒平均粒径为526.3nm,分散系数为0.288;制得的纳米粒对姜黄素具有良好的缓释作用。
关键词: 姜黄素;γ-聚谷氨酸;纳米颗粒;制备;缓释
Abstract
Nanoparticles were prepared using γ-polyglutamic acid(PGA), curcumin, and chitosan(CS) as matrix, polyvinylpyrrolidone(PVP) and sodium tripolyphosphate(STPP) as stabilizers and cross-linking agents. The optimal formula was determined by comparing the encapsulation rate, structural characterization and infrared spec- troscopy of curcumin in nanoparticles with different concentration ratio formulations; the in vitro release of nano- particles containing curcumin in two media were investigated by dynamic dialysis. The optimum formula for the production of curcumin nanoparticles were obtained as follows: curcumin concentration was 0.26mg/mL, PGA concentration was 0.2%, STPP concentration was 0.2%, PVP concentration was 0.1% and CS concentration was 0.02%(in 100mL aqueous solution). The average particle size of the nanoparticles was 526.3nm and the dispersion coefficient was 0.288. The prepared nanoparticles had a good slow release effect on curcumin.
Key words: Curcumin; γ-polyglutamic acid; Nanoparticles; Preparation; Slow release
参考文献 References
[1]刘伟,顾秀竹,吴筱霓,等. 姜黄素药理作用的研究进展[J].华西药学杂志,2021,36(03):336-340.
[2]张晓璐,李英鹏,吕邵娃,等. 姜黄素纳米载体与应用的研究进展[J].当代化工,2021,50(11):2685-2688.
[3]肖开兴,许引虎,王旭,等. CS在食品工业上的应用研究[J].酿酒科技,2021(10):71-75.
[4]沈一平. 聚氨基酸纳米递药系统构建及抗肿瘤作用研究[D].哈尔滨:哈尔滨商业大学,2020.
[5]赵倩. 基于金、银纳米簇构建化学/生物传感研究[D]. 湘潭: 湖南科技大学, 2015.
[6]谭少聪,邱梦辉,黄德金,等. 基于稳定剂和微胶囊化联用技术制备姜黄素纳米颗粒[J].食品研究与开发,2021,42(15):112-118.
[7]潘飞,赵磊,陈艳麟,等. CS/γ-聚谷氨酸负载黑米花色苷纳米粒的制备、表征及缓释性能[J].食品科学,2020,(07):1-12.
[8]Jong-Ho Kim et al. Hydrophobically modified glycol chitosan nanoparticles as carriers for paclitaxel[J]. Journal of Controlled Release, 2005,111(1):228-234.
[9]Tan QY, Wang N, Yang H, et al. Characterization, stabilization and activity of uricase loaded in lipid vesicles[J]. Int J Pharm, 2010,384(1-2):165-172.